US6787103B2 - Hydrogen storage alloy having laves phase and production method therefor - Google Patents

Hydrogen storage alloy having laves phase and production method therefor Download PDF

Info

Publication number
US6787103B2
US6787103B2 US10/012,497 US1249701A US6787103B2 US 6787103 B2 US6787103 B2 US 6787103B2 US 1249701 A US1249701 A US 1249701A US 6787103 B2 US6787103 B2 US 6787103B2
Authority
US
United States
Prior art keywords
hydrogen storage
storage alloy
production method
laves phase
alloy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime, expires
Application number
US10/012,497
Other versions
US20020046788A1 (en
Inventor
Yasuhiro Aoki
Takaaki Miyaki
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Japan Steel Works Ltd
Original Assignee
Japan Steel Works Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Japan Steel Works Ltd filed Critical Japan Steel Works Ltd
Assigned to JAPAN STEEL WORKS, LTD. reassignment JAPAN STEEL WORKS, LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AOKI, YASUHIRO, MIYAKI, TAKAAKI
Publication of US20020046788A1 publication Critical patent/US20020046788A1/en
Application granted granted Critical
Publication of US6787103B2 publication Critical patent/US6787103B2/en
Adjusted expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/0005—Reversible uptake of hydrogen by an appropriate medium, i.e. based on physical or chemical sorption phenomena or on reversible chemical reactions, e.g. for hydrogen storage purposes ; Reversible gettering of hydrogen; Reversible uptake of hydrogen by electrodes
    • C01B3/001—Reversible uptake of hydrogen by an appropriate medium, i.e. based on physical or chemical sorption phenomena or on reversible chemical reactions, e.g. for hydrogen storage purposes ; Reversible gettering of hydrogen; Reversible uptake of hydrogen by electrodes characterised by the uptaking medium; Treatment thereof
    • C01B3/0031—Intermetallic compounds; Metal alloys; Treatment thereof
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C22/00—Alloys based on manganese
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/383—Hydrogen absorbing alloys
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/32—Hydrogen storage
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S420/00—Alloys or metallic compositions
    • Y10S420/90—Hydrogen storage

Definitions

  • the present invention is based on Japanese Patent Application No. 2000-217187, which is incorporated herein by reference.
  • the present invention relates to a hydrogen storage alloy having a Laves phase containing vanadium.
  • the oxygen content of the raw materials, in particular, of the vanadium drastically influences the hydrogen absorbing and discharging performance.
  • the hydrogen absorbing amount of the alloy is deteriorated.
  • a vanadium has ordinarily a relatively large oxygen content of 10,000 ppm or more, a desired performance cannot be obtained in the case that the vanadium is directly used as the raw material for the hydrogen storage alloy. Therefore an oxygen reduction treatment is required. As a result, the alloy production cost is increased and a problem is caused that realization of a system containing the alloy is disturbed.
  • the heat treatment to be performed after forming the alloy also increases the production cost and the production time, Furthermore, it may lead to oxidization of the alloy so as to deteriorate the performance, and thus a problem of difficulty in handling is also involved.
  • an object of the invention is to provide a Ti—Zr—Mn—V—Fe hydrogen storage alloy with the excellent hydrogen absorbing and discharging performance by optimizing the components. Another object thereof is to provide a production method for a hydrogen storage alloy capable of producing the alloy efficiently at a low cost.
  • a first aspect of the invention is a hydrogen storage alloy having Laves phase represented by the general formula: Ti 1 ⁇ x Zr x Mn w ⁇ y ⁇ z V y Fe z , wherein 0 ⁇ x ⁇ 0.5, 0 ⁇ y ⁇ 0.6, 0 ⁇ z ⁇ 0.2, and 1.8 ⁇ w ⁇ 2.2.
  • a second aspect of the invention is the hydrogen storage alloy having a Laves phase according to the first aspect, wherein the content of the oxygen is 5,000 ppm or less.
  • a third aspect of the invention is a production method for a hydrogen storage alloy having a Laves phase, wherein the hydrogen storage alloy according to the first or second aspect is formed by using a ferrovanadium (alloy of a vanadium and an iron) as one of the raw materials.
  • a fourth aspect of the invention is the production method for a hydrogen storage alloy having a Laves phase according to the third aspect, wherein the oxygen content of the ferrovanadium is 4,000 ppm or less.
  • a fifth aspect of the invention is the production method for a hydrogen storage alloy having a Laves phase according to the third or fourth aspect, wherein the melted raw materials are rapidly quenched and solidified.
  • the titanium is an element capable of increasing the hydrogen absorbing amount, it is added as an essential component.
  • the atomic ratio should be 0.5 or more.
  • the hydrogen dissociation pressure is lowered. Therefore, the atomic ratio is set in the range of 0.5 to 1.0.
  • the zirconium is an element capable of adjusting the hydrogen equilibrium dissociation pressure, it is optionally added. However, in the case it is added by a more than 0.5 atomic ratio, the hydrogen equilibrium dissociation pressure is lowered. Therefore, the upper limit of the atomic ratio is set at 0.5.
  • the manganese is an element capable of lowering the hydrogenation reaction temperature, it is added as an essential component.
  • the atomic ratio should be 1.0 or more.
  • the hysteresis is enlarged. Therefore, the atomic ratio is set in the range of 1.0 to less than 2.2.
  • the vanadium is an element capable of increasing the hydrogen absorbing amount, it is added as an essential component. However, in the case it is added by a more than 0.6 atomic ratio, the reaction rate is lowered. Therefore, the upper limit of the atomic ratio is set at 0.6.
  • the iron is an element contained at the time of using a ferrovanadium, it is added as an essential component. However, in the case it is added by a more than 0.2 atomic ratio, the hydrogen equilibrium dissociation pressure is raised. Therefore, the upper limit of the atomic ratio is set at 0.2.
  • Impurity Oxygen 5,000 ppm or Less
  • the impurity oxygen contained in a hydrogen storage alloy influences the hydrogen absorbing and discharging ability. In the case the amount thereof is large, the absorbing and discharging ability is deteriorated. Therefore, the contained oxygen amount is preferably as little as possible. In consideration of the industrial applicability, the content thereof is preferably 5,000 ppm or less, and further preferably 1,000 ppm or less.
  • a hydrogen storage alloy according to the invention Since a hydrogen storage alloy according to the invention has a Laves phase structure, it provides a high hydrogen absorbing effect owing to the Laves structure.
  • the ferrovanadium can be used as the raw material. Since the ferrovanadium is produced at a low cost compared with the case of a vanadium single metal, a desired hydrogen storage alloy can be produced efficiently at a low cost.
  • the ferrovanadium for example, those containing a vanadium by 80 to 85% mass ratio, and an iron as the substantially remainder, can be presented.
  • the ferrovanadium has the oxygen included as the impurity, limited to 4,000 ppm or less. More preferably, the ferrovanadium may contain the oxygen not more than 3,000 ppm. According to the limitation of the oxygen content, the oxygen content of a hydrogen storage alloy prepared with the ferrovanadium as the raw material can be sufficiently lowered so that the averse effect to the hydrogen absorbing and discharging performance can be eliminated.
  • the raw materials with the components adjusted are melted, and rapidly quenched and solidified for preparation.
  • the plateau properties and the hysteresis properties can be improved dramatically so that the storage and transportation efficiency of the hydrogen can be improved.
  • the cooling operation at the time of forming an alloy is carried out by natural cooling or water cooling.
  • the above-mentioned effect can be formed by quenching and solidifying at a cooling rate higher than that of the conventional method.
  • the cooling rate a cooling rate of 100° C./second or more can be presented, and furthermore, a cooling rate of 10 3 ° C./second or more can be presented as a preferable embodiment.
  • the above-mentioned method for rapid solidification is not particularly limited, and various methods capable of obtaining the cooling rate can be adopted.
  • the gas atomize method, the centrifugal method, the rotation submerged jetting method, the roll quenching method, or the like can be adopted.
  • a hydrogen storage alloy is obtained preferably by measuring each of the Ti, Zr, Mn, Fe—V component materials so as to have the atomic ratio defined in the invention, melting the same by an ordinary method, and rapid solidification by the roll quenching method, or the like, as mentioned above.
  • the final alloy denotes an alloy in the state to be used for the targeted application without the need of a heat treatment, or the like.
  • the obtained hydrogen storage alloy is pulverized as needed by a mechanical method, or the like so as to provide a powdery hydrogen storage alloy.
  • the pulverization method is not particularly limited, and an optional method such as a known method can be adopted.
  • the hydrogen storage alloy in the powdery form can be used for a desired application as it is or after shaping.
  • the application of the hydrogen storage alloy obtained by the invention is not particularly limited, and it can be used for various applications utilizing the hydrogen absorbing and discharging phenomenon.
  • it can be used in a heat pump of a heat transportation system or a freezing system, a hydrogen storage system, or the like.
  • the hydrogen storage alloy obtained by the invention By use of the hydrogen storage alloy obtained by the invention in these systems, the system efficiency can be improved dramatically.
  • the elemental substances of Ti, Zr, and Mn and a ferrovanadium (V: about 85% by mass, Fe: about 15% by mass, and O: about 0.3% by mass) were used as the raw materials.
  • a hydrogen storage alloy was formed by melting the raw materials by the Ar arc melting, and quenching and solidifying the same by a single roll (average cooling rate 10 4 ° C./second).
  • the rechargeable hydrogen capacity at 40° C. was about a little less than 100 cc/g, and the contained oxygen amount in the alloy was 0.146% by mass.
  • the alloy raw material cost of the production of the hydrogen storage alloy was reduced by about 90% compared with the case of using the metal vanadium. Furthermore, it was learned that the excellent hydrogen absorbing and discharging performance can be provided.
  • the elemental substances were used for all of the components.
  • a hydrogen storage alloy was formed by melting the raw materials by the Ar arc melting, and quenching and solidifying the same by a single roll.
  • the contained oxygen amount of the V at the time was 14,000 ppm.
  • the rechargeable hydrogen capacity at 40° C. was about 100 cc/g, and the contained oxygen amount was 0.260% by mass.
  • the alloy production cost was lowered drastically.
  • the elemental substances were used for all of the components.
  • a hydrogen storage alloy was formed by melting the raw materials by the Ar arc melting, and applying a heat treatment in the Ar atmosphere at 1,100° C. for 24 hours. According to the result of the hydrogen pressure-composition-isothermal curve measurement, it was confirmed that a sufficient rechargeable hydrogen capacity cannot be ensured due to a large inclination in the plateau slope and the low heat treatment temperature compared with the case of the alloy produced by the single roll quenching and solidifying method.
  • the elemental substances of Ti, Zr, and Mn, and a ferrovanadium were used as the raw materials.
  • Hydrogen storage alloys with 0.8% by mass and 0.3% by mass contained oxygen amounts were obtained by melting the raw materials by the high frequency induction melting, and quenching and solidifying the same by a single roll. According to the result of the hydrogen pressure-composition-isothermal curve measurement, it was observed that the alloy with the 0.8% by mass contained oxygen amount has an rechargeable hydrogen capacity at 40° C. smaller by about 10 cc/g, and a raised plateau pressure.
  • a hydrogen storage alloy having Laves phase of the invention since it is represented by the general formula: Ti 1 ⁇ x Zr x Mn w ⁇ y ⁇ z V y Fe z , (wherein 0 ⁇ x ⁇ 0.5, 0 ⁇ y ⁇ 0.6, 0 ⁇ z ⁇ 0.2, and 1.8 ⁇ w ⁇ 2.2), the excellent hydrogen absorbing and discharging performance can be obtained by appropriately setting the components. According to the component setting, a hydrogen storage alloy can be formed using a relatively inexpensive ferrovanadium.
  • a hydrogen storage alloy with a small oxygen content can be formed from inexpensive materials so that a hydrogen storage alloy with the excellent hydrogen absorbing and discharging performance can be produced at a low cost.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Combustion & Propulsion (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Hydrogen, Water And Hydrids (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Continuous Casting (AREA)

Abstract

The present invention is to obtain a Ti—Zn—Mn—V—Fe based hydrogen storage alloy having the excellent hydrogen absorbing and discharging performance at a low cost. An alloy represented by the general formula: Ti1−xZrxMnw−y−zVyFez (wherein 0≦x≦0.5, 0<y≦0.6, 0<z≦0.2, and 1.8≦w≦2.2) is produced using a ferrovanadium (alloy of a V and an Fe) as one of the raw materials. The oxygen content of the alloy is limited to 5,000 ppm or less. A hydrogen storage alloy having the excellent hydrogen absorbing and discharging performance can be produced using an inexpensive ferrovanadium. Furthermore, an impurity oxygen, which adversely effect the performance, can be limited easily.

Description

CROSS REFERENCE TO RELATED APPLICATION
The present invention is based on Japanese Patent Application No. 2000-217187, which is incorporated herein by reference.
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a hydrogen storage alloy having a Laves phase containing vanadium.
2. Description of Related Art
Recently, hydrogen energy is focused as a new energy, and development of the hydrogen storage alloy reversibly absorbing and discharging hydrogen, is promoted elaborately in various fields, such as the hydrogen storage, heat pumps, actuators, and electrodes for secondary batteries. Among the hydrogen storage alloys, a Ti—Zr—Mn—V based hydrogen storage alloy has a large rechargeable hydrogen capacity, and the excellent alloy performance.
Conventionally, in order to obtain the alloy, a method of utilizing metals of elemental substances as the raw materials is applied, adjusting the component thereof at the time of melting, and providing the raw material melted mainly by the Ar arc melting method or the high frequency induction melting method into a dye. Moreover, after forming the alloy, a high temperature heat treatment is executed for a long time in order to improve the alloy performance.
In the above-mentioned Ti—Zr—Mn—V based hydrogen storage alloy, the oxygen content of the raw materials, in particular, of the vanadium drastically influences the hydrogen absorbing and discharging performance. In the case the content is large, the hydrogen absorbing amount of the alloy is deteriorated. However, since a vanadium has ordinarily a relatively large oxygen content of 10,000 ppm or more, a desired performance cannot be obtained in the case that the vanadium is directly used as the raw material for the hydrogen storage alloy. Therefore an oxygen reduction treatment is required. As a result, the alloy production cost is increased and a problem is caused that realization of a system containing the alloy is disturbed.
Moreover, the heat treatment to be performed after forming the alloy also increases the production cost and the production time, Furthermore, it may lead to oxidization of the alloy so as to deteriorate the performance, and thus a problem of difficulty in handling is also involved.
SUMMARY OF THE INVENTION
In view of the circumstances, an object of the invention is to provide a Ti—Zr—Mn—V—Fe hydrogen storage alloy with the excellent hydrogen absorbing and discharging performance by optimizing the components. Another object thereof is to provide a production method for a hydrogen storage alloy capable of producing the alloy efficiently at a low cost.
In order to solve the problems, a first aspect of the invention is a hydrogen storage alloy having Laves phase represented by the general formula: Ti1−xZrxMnw−y−zVyFez, wherein 0≦x≦0.5, 0<y≦0.6, 0<z≦0.2, and 1.8≦w≦2.2.
A second aspect of the invention is the hydrogen storage alloy having a Laves phase according to the first aspect, wherein the content of the oxygen is 5,000 ppm or less.
A third aspect of the invention is a production method for a hydrogen storage alloy having a Laves phase, wherein the hydrogen storage alloy according to the first or second aspect is formed by using a ferrovanadium (alloy of a vanadium and an iron) as one of the raw materials.
A fourth aspect of the invention is the production method for a hydrogen storage alloy having a Laves phase according to the third aspect, wherein the oxygen content of the ferrovanadium is 4,000 ppm or less.
A fifth aspect of the invention is the production method for a hydrogen storage alloy having a Laves phase according to the third or fourth aspect, wherein the melted raw materials are rapidly quenched and solidified.
Hereinafter, the atomic ratio defined in the invention, or the like, will be explained.
Atomic Ratio of the Alloy
Ti: Atomic Ratio 0.5 to 1.0
Since the titanium is an element capable of increasing the hydrogen absorbing amount, it is added as an essential component. However, in order to certainly obtain the above-mentioned effect, the atomic ratio should be 0.5 or more. In contrast, in the case it is added by more than a 1.0 amount, the hydrogen dissociation pressure is lowered. Therefore, the atomic ratio is set in the range of 0.5 to 1.0.
Zr: Atomic Ratio 0.5 or Less
Since the zirconium is an element capable of adjusting the hydrogen equilibrium dissociation pressure, it is optionally added. However, in the case it is added by a more than 0.5 atomic ratio, the hydrogen equilibrium dissociation pressure is lowered. Therefore, the upper limit of the atomic ratio is set at 0.5.
Mn: Atomic Ratio 1.0 to Less than 2.2
Since the manganese is an element capable of lowering the hydrogenation reaction temperature, it is added as an essential component. However, in order to certainly obtain the above-mentioned effect, the atomic ratio should be 1.0 or more. In contrast, in the case it is added by a 2.2 or more amount, the hysteresis is enlarged. Therefore, the atomic ratio is set in the range of 1.0 to less than 2.2.
V: Atomic Ratio 0.6 or Less
Since the vanadium is an element capable of increasing the hydrogen absorbing amount, it is added as an essential component. However, in the case it is added by a more than 0.6 atomic ratio, the reaction rate is lowered. Therefore, the upper limit of the atomic ratio is set at 0.6.
Fe: Atomic Ratio 0.2 or Less
Since the iron is an element contained at the time of using a ferrovanadium, it is added as an essential component. However, in the case it is added by a more than 0.2 atomic ratio, the hydrogen equilibrium dissociation pressure is raised. Therefore, the upper limit of the atomic ratio is set at 0.2.
Impurity Oxygen: 5,000 ppm or Less
The impurity oxygen contained in a hydrogen storage alloy influences the hydrogen absorbing and discharging ability. In the case the amount thereof is large, the absorbing and discharging ability is deteriorated. Therefore, the contained oxygen amount is preferably as little as possible. In consideration of the industrial applicability, the content thereof is preferably 5,000 ppm or less, and further preferably 1,000 ppm or less.
Laves Phase
Since a hydrogen storage alloy according to the invention has a Laves phase structure, it provides a high hydrogen absorbing effect owing to the Laves structure.
Use of Ferrovanadium
Since the alloy of the invention provides a good hydrogen absorbing and discharging performance owing to an appropriate component adjustment (including the iron), the ferrovanadium can be used as the raw material. Since the ferrovanadium is produced at a low cost compared with the case of a vanadium single metal, a desired hydrogen storage alloy can be produced efficiently at a low cost. As the ferrovanadium, for example, those containing a vanadium by 80 to 85% mass ratio, and an iron as the substantially remainder, can be presented. Furthermore, it is desirable that the ferrovanadium has the oxygen included as the impurity, limited to 4,000 ppm or less. More preferably, the ferrovanadium may contain the oxygen not more than 3,000 ppm. According to the limitation of the oxygen content, the oxygen content of a hydrogen storage alloy prepared with the ferrovanadium as the raw material can be sufficiently lowered so that the averse effect to the hydrogen absorbing and discharging performance can be eliminated.
Rapid Solidification
Furthermore, in the production of a hydrogen storage alloy according to the invention, the raw materials with the components adjusted, are melted, and rapidly quenched and solidified for preparation.
By preparing the hydrogen storage alloy by quenching and solidifying, by for example, roll quenching, the plateau properties and the hysteresis properties can be improved dramatically so that the storage and transportation efficiency of the hydrogen can be improved. In the conventional production method, the cooling operation at the time of forming an alloy is carried out by natural cooling or water cooling. In contrast, in the invention, the above-mentioned effect can be formed by quenching and solidifying at a cooling rate higher than that of the conventional method. As to the cooling rate, a cooling rate of 100° C./second or more can be presented, and furthermore, a cooling rate of 103° C./second or more can be presented as a preferable embodiment.
Particularly in the case of adding a zirconium, segregation of the zirconium in the alloy can be prevented so that a problem of increase of the plateau slope due to the zirconium segregation can be solved.
The above-mentioned method for rapid solidification is not particularly limited, and various methods capable of obtaining the cooling rate can be adopted. For example, the gas atomize method, the centrifugal method, the rotation submerged jetting method, the roll quenching method, or the like, can be adopted.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
In the invention, a hydrogen storage alloy is obtained preferably by measuring each of the Ti, Zr, Mn, Fe—V component materials so as to have the atomic ratio defined in the invention, melting the same by an ordinary method, and rapid solidification by the roll quenching method, or the like, as mentioned above.
Although a homogenization process of heating the alloy at a high temperature for homogenizing the components is applied in the conventional method after preparing a hydrogen storage alloy, in the invention, a sufficient homogenization effect is obtained by the above-mentioned rapid solidification so that a final alloy can be provided without the need of the homogenization process, which is executed in the conventional method. The final alloy denotes an alloy in the state to be used for the targeted application without the need of a heat treatment, or the like.
The obtained hydrogen storage alloy is pulverized as needed by a mechanical method, or the like so as to provide a powdery hydrogen storage alloy. The pulverization method is not particularly limited, and an optional method such as a known method can be adopted.
The hydrogen storage alloy in the powdery form can be used for a desired application as it is or after shaping. The application of the hydrogen storage alloy obtained by the invention is not particularly limited, and it can be used for various applications utilizing the hydrogen absorbing and discharging phenomenon. For example, it can be used in a heat pump of a heat transportation system or a freezing system, a hydrogen storage system, or the like. By use of the hydrogen storage alloy obtained by the invention in these systems, the system efficiency can be improved dramatically.
EXAMPLES
Hereinafter, the example of the invention will be explained in comparison with the comparative examples.
Embodiment
In order to obtain the alloy composition Ti0.7Zr0.3Mn1.4V0.5Fe0.1, the elemental substances of Ti, Zr, and Mn and a ferrovanadium (V: about 85% by mass, Fe: about 15% by mass, and O: about 0.3% by mass) were used as the raw materials. A hydrogen storage alloy was formed by melting the raw materials by the Ar arc melting, and quenching and solidifying the same by a single roll (average cooling rate 104° C./second).
According to the hydrogen pressure-composition-isothermal curve measurement (PCT curve measurement) and the component analysis of the alloy, it was found out that the rechargeable hydrogen capacity at 40° C. was about a little less than 100 cc/g, and the contained oxygen amount in the alloy was 0.146% by mass. The alloy raw material cost of the production of the hydrogen storage alloy was reduced by about 90% compared with the case of using the metal vanadium. Furthermore, it was learned that the excellent hydrogen absorbing and discharging performance can be provided.
Comparative Example 1
In order to obtain the alloy composition Ti0.7Zr0.3Mn1.4V0.5Fe0.1, the elemental substances were used for all of the components. A hydrogen storage alloy was formed by melting the raw materials by the Ar arc melting, and quenching and solidifying the same by a single roll. The contained oxygen amount of the V at the time was 14,000 ppm. According to the hydrogen pressure-composition-isothermal curve measurement and the component analysis of the alloy, it was found out that the rechargeable hydrogen capacity at 40° C. was about 100 cc/g, and the contained oxygen amount was 0.260% by mass. In the comparative example 1, the alloy production cost was soared drastically.
Comparative Example 2
In order to obtain the alloy composition Ti0.7Zr0.3Mn1.4V0.5Fe0.1, the elemental substances were used for all of the components. A hydrogen storage alloy was formed by melting the raw materials by the Ar arc melting, and applying a heat treatment in the Ar atmosphere at 1,100° C. for 24 hours. According to the result of the hydrogen pressure-composition-isothermal curve measurement, it was confirmed that a sufficient rechargeable hydrogen capacity cannot be ensured due to a large inclination in the plateau slope and the low heat treatment temperature compared with the case of the alloy produced by the single roll quenching and solidifying method.
Comparative Example 3
In order to obtain the alloy composition Ti0.7Zr0.3Mn1.4V0.5Fe0.1, the elemental substances of Ti, Zr, and Mn, and a ferrovanadium were used as the raw materials. Hydrogen storage alloys with 0.8% by mass and 0.3% by mass contained oxygen amounts were obtained by melting the raw materials by the high frequency induction melting, and quenching and solidifying the same by a single roll. According to the result of the hydrogen pressure-composition-isothermal curve measurement, it was observed that the alloy with the 0.8% by mass contained oxygen amount has an rechargeable hydrogen capacity at 40° C. smaller by about 10 cc/g, and a raised plateau pressure.
As heretofore explained, according to a hydrogen storage alloy having Laves phase of the invention, since it is represented by the general formula: Ti1−xZrxMnw−y−zVyFez, (wherein 0≦x≦0.5, 0<y≦0.6, 0<z≦0.2, and 1.8≦w≦2.2), the excellent hydrogen absorbing and discharging performance can be obtained by appropriately setting the components. According to the component setting, a hydrogen storage alloy can be formed using a relatively inexpensive ferrovanadium.
Moreover, by setting the oxygen content of the ferrovanadium at not more than 4,000 ppm (preferably not more than 3,000 ppm), a hydrogen storage alloy with a small oxygen content can be formed from inexpensive materials so that a hydrogen storage alloy with the excellent hydrogen absorbing and discharging performance can be produced at a low cost.

Claims (18)

What is claimed is:
1. A production method for a hydrogen storage alloy having a Laves phase represented by the general formula: Ti1−xZrxMnw−y−zVyFez, wherein 0≦x≦0.5, 0<y≦0.6, 0<z≦0.2, and 1.8≦w≦2.2,
comprising forming said hydrogen storage alloy by melting raw materials, wherein said raw materials comprise an alloy comprising a vanadium and an iron.
2. The production method for a hydrogen storage alloy having a Laves phase according to claim 1, wherein said alloy comprising a vanadium and an iron is a ferrovanadium and the oxygen content of the ferrovanadium is not more than 4,000 ppm.
3. The production method for a hydrogen storage alloy having Laves phase according to claim 1, wherein the melted raw materials are rapidly quenched and solidified.
4. The production method for a hydrogen storage alloy having a Laves phase according to claim 1, wherein a titanium, a zirconium, a manganese and a ferrovanadium are provided separately in said raw materials and said raw materials are melted by Ar arc melting and integrated into said hydrogen storage alloy.
5. The production method for a hydrogen storage alloy having a Laves phase according to claim 2, wherein the ferrovanadium includes 80 to 85% by mass ratio of vanadium and the remainder being substantially iron.
6. The production method for a hydrogen storage alloy having a Laves phase according to claim 3, wherein the melted material is rapidly quenched with cooling rate about 104° C./second.
7. A production method for a hydrogen storage ally having a Laves phase represented by the general formula: Ti1−xZrxMnw−y−zVyFez, wherein 0≦x≦0.5, 0<y≦0.6, 0<z≦0.2, and 1.8≦w≦2.2, said production method comprising the steps of:
providing separately a titanium, a zirconium, and a manganese as raw materials;
providing a ferrovanadium as another raw material;
integrally melting the titanium, the zirconium, the manganese and the ferrovanadium;
quenching and solidifying the melted raw materials.
8. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, wherein the oxygen content of the ferrovanadium is not more than 4,000 ppm.
9. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, wherein the ferrovanadium includes 80 to 85% by mass ratio of vanadium and the remainder being substantially iron.
10. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, wherein the melted material is rapidly quenched with cooling rate about 104° C./second.
11. The production method for a hydrogen storage alloy having a Laves phase according to claim 3, wherein said quenching is roll quenching.
12. The production method for a hydrogen storage alloy having a Laves phase according to claim 3, wherein the melted material is rapidly quenched at a cooling rate of 103° C./second or more.
13. The production method for a hydrogen storage alloy having a Laves phase according to claim 1, further comprising pulverizing the hydrogen storage alloy.
14. The production method for a hydrogen storage alloy having a Laves phase according to claim 2, wherein the oxygen content of the ferrovanadium is not more than 3,000 ppm.
15. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, wherein said quenching is roll quenching.
16. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, wherein the melted material is rapidly quenched at a cooling rate of 103° C./second or more.
17. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, further comprising pulverizing the hydrogen storage alloy.
18. The production method for a hydrogen storage alloy having a Laves phase according to claim 7, wherein the oxygen content of the ferrovanadium is not more than 3,000 ppm.
US10/012,497 2000-07-18 2001-12-12 Hydrogen storage alloy having laves phase and production method therefor Expired - Lifetime US6787103B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2000-217187 2000-07-18
JP2000217187A JP2002030371A (en) 2000-07-18 2000-07-18 Laves phase hydrogen storage alloy and method for producing the same alloy
DE10162232A DE10162232A1 (en) 2000-07-18 2001-12-18 Laves phased hydrogen occluding titanium-zirconium-manganese-vanadium-iron system alloy

Publications (2)

Publication Number Publication Date
US20020046788A1 US20020046788A1 (en) 2002-04-25
US6787103B2 true US6787103B2 (en) 2004-09-07

Family

ID=28676022

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/012,497 Expired - Lifetime US6787103B2 (en) 2000-07-18 2001-12-12 Hydrogen storage alloy having laves phase and production method therefor

Country Status (3)

Country Link
US (1) US6787103B2 (en)
JP (1) JP2002030371A (en)
DE (1) DE10162232A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112030054A (en) * 2020-09-09 2020-12-04 中南大学 TiZrMnFe quaternary getter alloy material and preparation method and application thereof
CN117286378A (en) * 2023-09-27 2023-12-26 承德天大钒业有限责任公司 TiMnV-based hydrogen storage alloy and preparation method and application thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0210659A (en) 1988-06-28 1990-01-16 Matsushita Electric Ind Co Ltd Manufacture of hydrogen storage alloy
US4946646A (en) * 1987-05-15 1990-08-07 Matsushita Electric Industrial Co., Ltd. Alloy for hydrogen storage electrodes
US5281390A (en) * 1988-06-28 1994-01-25 Matsushita Electric Industrial Co., Ltd. Method of producing hydrogen-storing alloy and electrode making use of the alloy
US5490970A (en) * 1988-06-28 1996-02-13 Matsushita Electric Industrial Co., Ltd. Method of producing hydrogen-storing alloy and electrode making use of the alloy
US5552246A (en) * 1994-03-14 1996-09-03 Hong; Kuochih Materials for hydrogen storage, hydride electrodes and hydride batteries
US5695530A (en) * 1994-03-14 1997-12-09 Hong; Kuochih Method for making high charging efficiency and fast oxygen recombination rechargeable hydride batteries
DE19916614A1 (en) 1998-05-21 1999-12-02 Toyota Motor Co Ltd Low cost hydrogen absorbent alloy used in hydrogen storage and transport devices and cells
DE10108654A1 (en) 2000-02-22 2001-09-13 Japan Steel Works Ltd Production of a hydrogen storage alloy having a structure with a hexagonal packing comprises rapidly solidifying a molten starting material to obtain the storage alloy
US6626323B2 (en) * 2002-02-21 2003-09-30 Energy Conversion Devices, Inc. Vane heat transfer structure

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3210381C1 (en) * 1982-03-20 1983-05-19 Daimler-Benz Ag, 7000 Stuttgart Alloy for storing hydrogen
DE3411011C2 (en) * 1984-03-24 1986-04-03 GfE Gesellschaft für Elektrometallurgie mbH, 4000 Düsseldorf Process for producing a titanium-containing hydrogen storage alloy
JPH06228687A (en) * 1993-01-29 1994-08-16 Daido Steel Co Ltd Hydrogen storage alloy and its production
JPH0949034A (en) * 1995-08-10 1997-02-18 Matsushita Electric Ind Co Ltd Production of hydrogen storage alloy
JPH11106847A (en) * 1997-10-02 1999-04-20 Imura Zairyo Kaihatsu Kenkyusho:Kk Production of hydrogen storage alloy, alloy thereof and electrode using the alloy

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4946646A (en) * 1987-05-15 1990-08-07 Matsushita Electric Industrial Co., Ltd. Alloy for hydrogen storage electrodes
JPH0210659A (en) 1988-06-28 1990-01-16 Matsushita Electric Ind Co Ltd Manufacture of hydrogen storage alloy
US5281390A (en) * 1988-06-28 1994-01-25 Matsushita Electric Industrial Co., Ltd. Method of producing hydrogen-storing alloy and electrode making use of the alloy
US5490970A (en) * 1988-06-28 1996-02-13 Matsushita Electric Industrial Co., Ltd. Method of producing hydrogen-storing alloy and electrode making use of the alloy
US5552246A (en) * 1994-03-14 1996-09-03 Hong; Kuochih Materials for hydrogen storage, hydride electrodes and hydride batteries
US5695530A (en) * 1994-03-14 1997-12-09 Hong; Kuochih Method for making high charging efficiency and fast oxygen recombination rechargeable hydride batteries
DE19916614A1 (en) 1998-05-21 1999-12-02 Toyota Motor Co Ltd Low cost hydrogen absorbent alloy used in hydrogen storage and transport devices and cells
DE10108654A1 (en) 2000-02-22 2001-09-13 Japan Steel Works Ltd Production of a hydrogen storage alloy having a structure with a hexagonal packing comprises rapidly solidifying a molten starting material to obtain the storage alloy
US6626323B2 (en) * 2002-02-21 2003-09-30 Energy Conversion Devices, Inc. Vane heat transfer structure

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Japanese Patent Abstract No. 02010659, dated Jan. 16, 1990.

Also Published As

Publication number Publication date
DE10162232A1 (en) 2003-07-10
US20020046788A1 (en) 2002-04-25
JP2002030371A (en) 2002-01-31

Similar Documents

Publication Publication Date Title
US9850562B2 (en) Fe-based nano-crystalline alloy
US4093454A (en) Nickel-base sintered alloy
US5989491A (en) Oxide dispersion strengthened heat resisting powder metallurgy alloy and process for producing the same
US4681623A (en) Process for producing alloy powder containing rare earth metals
JPH068484B2 (en) Article made from processable boron-containing stainless steel alloy and method of making the same
US7413589B2 (en) Method of producing hydrogen storage alloy
JP6164387B1 (en) Method for producing alloy steel powder for sintered member raw material
JPH10102105A (en) Manufacture of fine metallic powder
US6419764B1 (en) Hydrogen storage material
US6787103B2 (en) Hydrogen storage alloy having laves phase and production method therefor
JP4515548B2 (en) Bulk amorphous alloy and high strength member using the same
JP3352965B2 (en) Zinc alloy powder for alkaline batteries with low gas generation
JP3845057B2 (en) Hydrogen storage alloy and heat treatment method of hydrogen storage alloy
EP3266887A1 (en) Thin titanium sheet and manufacturing method therefor
EP1793007B1 (en) Method for producing unidirectionally solidified hydrogen storage alloy
CN114000030B (en) Titanium-chromium-manganese hydrogen storage alloy and preparation method and application thereof
CN112593135B (en) Low-vanadium hydrogen storage alloy and preparation method and application thereof
EP1055740B1 (en) Hydrogen storage alloy and method for preparation thereof
JPS5839222B2 (en) Manufacturing method of wear-resistant sintered alloy
JP2002030374A (en) Hydrogen storage alloy and its production method
WO2002042507A1 (en) Hydrogen-occluding alloy and method for production thereof
CN114672740B (en) Yttrium-iron-based hydrogen storage alloy, battery and preparation method
JP4524384B2 (en) Quasicrystal-containing titanium alloy and method for producing the same
CA2521694C (en) Hydrogen storage alloy material and process for producing the same
JP3321818B2 (en) Method for producing hydrogen storage alloy for Ni-hydrogen battery

Legal Events

Date Code Title Description
AS Assignment

Owner name: JAPAN STEEL WORKS, LTD., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:AOKI, YASUHIRO;MIYAKI, TAKAAKI;REEL/FRAME:012379/0082

Effective date: 20011203

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCF Information on status: patent grant

Free format text: PATENTED CASE

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12